EP1762176B1 - Dispositif de tomographie aux rayons x - Google Patents

Dispositif de tomographie aux rayons x Download PDF

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Publication number
EP1762176B1
EP1762176B1 EP06018572.5A EP06018572A EP1762176B1 EP 1762176 B1 EP1762176 B1 EP 1762176B1 EP 06018572 A EP06018572 A EP 06018572A EP 1762176 B1 EP1762176 B1 EP 1762176B1
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EP
European Patent Office
Prior art keywords
ray
heart rate
scanning
period
projection data
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EP06018572.5A
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German (de)
English (en)
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EP1762176A3 (fr
EP1762176A2 (fr
Inventor
Kiyoshi Nagata
Masaharu Tsuyuki
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Canon Medical Systems Corp
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Toshiba Medical Systems Corp
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Priority to EP12152083.7A priority Critical patent/EP2449968B1/fr
Priority to EP10170123.3A priority patent/EP2238906B1/fr
Priority to EP12152086A priority patent/EP2449969A1/fr
Priority to EP12152088.6A priority patent/EP2449970B1/fr
Priority to EP12152080.3A priority patent/EP2452626B1/fr
Publication of EP1762176A2 publication Critical patent/EP1762176A2/fr
Publication of EP1762176A3 publication Critical patent/EP1762176A3/fr
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00—Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment
    • A61B6/54—Control of apparatus or devices for radiation diagnosis
    • A61B6/541—Control of apparatus or devices for radiation diagnosis involving acquisition triggered by a physiological signal
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00—Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment
    • A61B6/02—Devices for diagnosis sequentially in different planes; Stereoscopic radiation diagnosis
    • A61B6/03—Computerised tomographs
    • A61B6/032—Transmission computed tomography [CT]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00—Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment
    • A61B6/40—Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment with arrangements for generating radiation specially adapted for radiation diagnosis
    • A61B6/405—Source units specially adapted to modify characteristics of the beam during the data acquisition process
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00—Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment
    • A61B6/50—Clinical applications
    • A61B6/503—Clinical applications involving diagnosis of heart
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00—Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment
    • A61B6/54—Control of apparatus or devices for radiation diagnosis
    • A61B6/542—Control of apparatus or devices for radiation diagnosis involving control of exposure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/024—Detecting, measuring or recording pulse rate or heart rate
    • A61B5/0245—Detecting, measuring or recording pulse rate or heart rate by using sensing means generating electric signals, i.e. ECG signals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00—Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment
    • A61B6/02—Devices for diagnosis sequentially in different planes; Stereoscopic radiation diagnosis
    • A61B6/027—Devices for diagnosis sequentially in different planes; Stereoscopic radiation diagnosis characterised by the use of a particular data acquisition trajectory, e.g. helical or spiral

Definitions

  • the present invention relates to an X-ray computed tomography apparatus which can perform ECG gated reconstruction.
  • An X-ray computed tomography apparatus provides information about a subject to be examined in the form of images on the basis of the intensities of X-rays transmitted through the subject, and serves as an important role in many medical activities such as disease diagnosis, medical treatment, and surgical operation planning.
  • ECG gated scanning is performed to acquire ECG gated signals (trigger signals and R wave signals) and electrocardiographic signals (ECG signals) in parallel with scanning and obtain an image synchronous with a cardiac phase by using the electrocardiographic waveform signals or the like after data acquisition.
  • ECG gated scanning is performed to acquire ECG gated signals (trigger signals and R wave signals) and electrocardiographic signals (ECG signals) in parallel with scanning and obtain an image synchronous with a cardiac phase by using the electrocardiographic waveform signals or the like after data acquisition.
  • Recent cardiac examination attempts to reduce exposure by applying X-rays only in a specific phase by using electrocardiographic information.
  • an X-ray application period at the time of scanning is determined by using an R-R wave interval (cardiac cycle) corresponding to one heartbeat which is acquired before scanning.
  • This technique may be applicable to a heart phantom with a constant cardiac cycle.
  • the actual cardiac cycle of a subject (patient) is unstable, and a cardiac cycle corresponding to several heartbeats is not constant even before scanning. It is therefore not practical to determine an X-ray application period by using only a cardiac cycle corresponding to one heartbeat.
  • an X-ray computed tomography apparatus provides information about a subject to be examined in the form of images on the basis of the intensities of X-rays transmitted through the subject, and serves as an important role in many medical activities such as disease diagnosis, medical treatment, and surgical operation planning.
  • examination of a fast-moving part using an X-ray computed tomography apparatus, and in particular, cardiac examination one of the important challenges is to improve the time resolution of images.
  • a direct method of achieving this challenge is to shorten the time taken for one rotation of an X-ray tube, i.e., to speed up scanning.
  • Speeding up scanning makes a so-called ECG gated scanning method effectively function, which acquires only data in a specific period in a cardiac cycle by performing scanning in synchronism with an electrocardiogram.
  • X-ray are generated only in a specific period or the intensity of X-rays is increased in a specific period. This makes it possible to reduce an exposure dose as compared with a case wherein X-rays are continuously applied.
  • US 6 298 111 B1 relates to an X-ray computer tomography apparatus for reconstructing an image, i.e., a tomogram, of a slice of an inner portion of a subject on the basis of projection data on the subject in many directions.
  • WO 01/43462 A2 relates to medical diagnostic cardiac imaging, in particular to computer tomography (CT) scanners.
  • CT computer tomography
  • US 6 504 893 B1 relates to a method for examining a body region executing a periodic motion in an examination subject by means of computer tomography (CT) apparatus of the type having an X-ray source continuously rotating around a system axis and from which an X-ray beam penetrating the examination subject proceeds, and having a detector system for the X-rays emanating from the X-ray source that has at least a first detector line and a last detector line, wherein the examination subject, and the X-ray source and the detector system, are displaced relative to one another in the radial direction of the system axis during the rotation of the X-ray source, and wherein a tomogram of at least the body region executing the periodic motion is determined with an electronic calculating means from the output data of the detector system corresponding to the detected X-rays.
  • CT computer to
  • US 6 708 052 B1 relates generally to cardiac imaging and, in particular, acquiring cardiac images having minimized motion artifact with high-speed imaging devices.
  • the document relates to a method and apparatus for acquiring these cardiac images by prospective gating based in part on the length of a cardiac cycle, gender of the subject being imaged and the imaging speed. It is an object of the present invention to prevent the omission of part of projection data required for image reconstruction in an X-ray computed tomography apparatus which can perform ECG gated reconstruction. This is achieved by the X-ray computed tomography apparatus according to claim 1. Further advantageous embodiments are defined in the dependent claims.
  • X-ray computed tomography apparatuses include various types of apparatuses, e.g., a rotate/rotate-type apparatus in which an X-ray tube and X-ray detector rotate together around a subject to be examined, and a stationary/rotate-type apparatus in which many detection elements are arrayed in the form of a ring or plane, and only an X-ray tube rotates around a subject to be examined.
  • the present invention can be applied to either type. In this case, the rotate/rotate type, which is currently the mainstream, will be exemplified.
  • projection data corresponding to one rotation around a subject to be examined i.e., about 360°
  • projection data corresponding to 180° + ⁇ ⁇ : fan angle
  • This embodiment uses the half reconstruction method effective for imaging the heart with fast movement or the like.
  • an indirect conversion type that converts X-rays into light through a phosphor such as a scintillator and converts the light into electric charges through photoelectric conversion elements such as photodiodes
  • a direct conversion type that uses generation of electron-hole pairs in a semiconductor by X-rays and migration of the electron-hole pairs to an electrode, i.e., a photoconductive phenomenon.
  • the former type i.e., the indirect conversion type
  • the present invention can be applied to both a single-tube type X-ray computed tomography apparatus and a multi-tube type X-ray computed tomography apparatus.
  • the single-tube type X-ray computed tomography apparatus will be exemplified here.
  • FIG. 1 shows the schematic arrangement of the X-ray computed tomography apparatus according to this embodiment.
  • This X-ray computed tomography apparatus comprises a gantry device (scanning unit) 1 which acquires projection data associated with a subject (patient) P, a bed device 3 on which the subject P is placed, and a console 2 which controls the gantry device 1 and the bed device 3 and performs image reconstruction processing, image display, and the like based on the data acquired by the gantry device 1.
  • the gantry device 1 comprises a housing accommodating an X-ray tube 101, X-ray detector 102, rotating frame 103, high voltage generator 104, gantry driving device 105, and data acquisition device 107.
  • the housing has an opening portion for diagnosis in which the subject P is inserted.
  • the X-ray tube 101 and the X-ray detector 102 are mounted on the ring-like rotating frame 103 which is rotated/driven by the gantry driving device 105.
  • the rotation axis of the rotating frame 103 is defined as the Z-axis.
  • an axis perpendicular to the Z-axis which connects the focal point of the X-ray tube 101 and the center of the detection surface of the X-ray detector 102 is defined as the X-axis.
  • the Y-axis is perpendicular to both the Z-axis and the X-axis.
  • the rotating frame 103 is rotated by the gantry driving device 105 under the control of a scanning control unit 201.
  • the X-ray tube 101 and the X-ray detector 102 rotate around the subject P.
  • the X-ray tube 101 generates X-rays.
  • the X-rays generated from the X-ray tube 101 and transmitted through the subject are detected by the X-ray detector 102 and are acquired as projection data by the data acquisition device 107.
  • a top 302 of the bed device 3 is moved by a bed driving device 301.
  • the scanning control unit 201 controls the rotation of the rotating frame 103 and the movement of the top 302. This control allows the top 302 to make continuous movement synchronously during constant rotation of the rotating frame 103. This makes it possible to realize so-called helical scanning of moving the X-ray tube 101 (X-ray source) helically relative to the subject P and acquiring projection data at a plurality of positions on the helical path.
  • This embodiment will exemplify a case wherein projection data obtained by multi-helical scanning which is a technique of simultaneously acquiring data by using a multi-row detector.
  • this embodiment is also applicable to so-called dynamic scanning of continuously acquiring projection data while the top 302 is at rest or conventional scanning of repeating the operation of acquiring projection data corresponding to one rotation while the top 302 is at rest at a given position and acquiring projection data corresponding to one rotation at the next position after the top 302 is moved and stopped.
  • the rotating frame 103 has an opening portion in its central portion like the housing.
  • An electrocardiograph 106 serves to detect an electrocardiographic signal from an electrode attached to the subject P.
  • the electrocardiograph 106 detects a weak current generated from the heart of the subject P and outputs a temporal change in detected current as an electrocardiogram.
  • a system control unit 212 obtains a heart rate on the basis of the electrocardiographic information (P wave, Q wave, R wave, S wave, or T wave; R wave in this embodiment) obtained by the electrocardiograph 106.
  • the electrocardiograph 106 may acquire electrocardiographic information, and the system control unit 212 may obtain an electrocardiogram and a heart rate.
  • FIG. 1 shows the electrocardiograph 106 as part of the gantry device 1.
  • the electrocardiograph 106 may be configured independently of the gantry device 1, and it suffices to have a function of acquiring electrocardiographic information or electrocardiographic signals from the electrocardiograph 106 and a function of storing the electrocardiographic signals in a storage unit such as a projection data storage unit 203.
  • the high voltage generator 104 applies a tube voltage between the cathode and anode of the X-ray tube 101.
  • the high voltage generator 104 also supplies a filament current (tube current) to the filament of the X-ray tube 101.
  • X-rays are generated from the target of the anode of the X-ray tube 101 by the application of the tube voltage and the supply of the filament current.
  • the X-ray detector 102 is used to detect X-rays transmitted through the subject P.
  • a multi-slice type detector or a single-slice type detector may be used.
  • the X-ray detector 102 will be described as a multi-slice type detector which exhibits a high exposure reducing effect than an X-ray modulation function (to be described later).
  • the X-ray detector 102 is provided with pluralities of detection elements for detecting X-rays which are arranged in the channel direction (approximated to the Y-axis direction) and the slice direction (Z-axis direction) of the subject, respectively.
  • a plurality of X-ray detection elements e.g., about 600 to 1,000 detection elements, are arranged in the channel direction, and about 24 to 256 rows of detection elements are arranged side by side in the slice direction.
  • a multi-row detector is used, in which a plurality of X-ray detection elements each having a 0.5 mm ⁇ 0.5 mm square light-receiving surface are arranged such that 1,000 elements are arranged in the channel direction, and 64 rows of elements are arranged in the slice direction.
  • Each detection element includes a scintillator and a photodiode chip (not shown).
  • the X-ray detector 102 may either be a multi-slice type detector having detection elements with an equal size arranged in the slice direction or a multi-slice type detector having a plurality of detection elements with different sizes arranged in the slice direction at uneven pitches.
  • a data acquisition device (DAS (Data Acquisition System)) 107 converts a signal output from the X-ray detector 102 for each channel into a voltage signal, amplifies it, and further converts it into a digital signal.
  • This data also called pure raw data
  • a pre-processing unit 202 of the console 2 performs correction processing such as offset correction, reference correction, and sensitivity correction for the data (pure raw data) output from the data acquisition device 107.
  • the pre-processed pure raw data is generally called raw data. In this case, pure raw data and raw data will be genetically called "projection data".
  • Projection data is stored in the projection data storage unit 203 of the console 2, together with the electrocardiographic data obtained by the electrocardiograph 106, while codes representing a view representing the rotation angle of the X-ray tube 101 at the time of data acquisition, a channel number, and a row number (the position of the top 302 in some case) are associated with each other.
  • the projection data and the electrocardiographic signal (or electrocardiographic information) are associated with each other (or synchronized witch each other according to a person skilled in the art).
  • the projection data and the electrocardiographic signal may be stored physically or individually stored in one or more storage media. Alternatively, one storage medium may have different storage areas for the projection data and the electrocardiographic signal.
  • the console 2 includes the scanning control unit 201, an image reconstruction processing unit 206, an examination plan setting unit 207, an image storage unit 209, a display unit 210, and the system control unit 212 in addition to the pre-processing unit 202 and the projection data storage unit 203.
  • the image reconstruction processing unit 206 performs ECG gated reconstruction on the basis of the electrocardiographic signal (or the heart rate obtained by the system control unit 212) and projection data stored in the projection data storage unit 203.
  • the image reconstruction processing unit 206 comprises a half reconstruction function as an ECG gated reconstruction function and a segment reconstruction function.
  • a projection data group comprises a plurality of projection data sets (also referred to as a plurality of segments).
  • the plurality of projection data respectively correspond to a plurality of cardiac cycles.
  • Each of the plurality of projection data sets is a set of projection data acquired within a specific period having a predetermined time width which is centered on a specific cardiac phase (reconstruction central phase) designated by the examination plan setting unit 207.
  • three projection data sets acquired within a predetermined period centered on a cardiac phase of 65% are selected from three continuous or discrete cardiac cycles.
  • the three projection data sets covers 180° + fan angle.
  • the image reconstruction processing unit 206 weights and adds the projection data of one segment and the projection data of the other segment for each view instead of selecting one of the projection data for each view.
  • Weights are relatively determined in accordance with heart rates. As the heart rate decreases, a higher weight is attached, and vice versa. This makes it possible to reduce motion artifact. For example, weights are determined by the following equation.
  • the weight WA for the projection data of the segment A is 0.45
  • the weight WB for the projection data of the segment B is 0.55.
  • a weight need not always correspond to a heart rate.
  • a weight is made to correspond to the occupation ratio of each projection data set to the angle range of (180 + ⁇ ) which is required for image reconstruction.
  • a weight to be applied to projection data in a projection data set exhibiting a relatively high occupation ratio is set to be higher than that applied to projection data in a projection data set exhibiting a relatively low occupation ratio. If, for example, the heart rate at the time of acquisition of the segment A is 90 bps and the heart rate at the time of acquisition of the segment B is 75 bps, the weight WA for the projection data of the segment is set to 0.3, and the weight WB for the projection data of the segment is set to 0.7.
  • the number of segments for segment reconstruction may be set by the examination plan setting unit 207. Assume, however, that the number of segments is automatically determined on the basis of the average heart rate acquired from the electrocardiograph 106 (or the storage unit 203) or the average heart rate and scanning speed (the rotational speed of the rotating frame 103) acquired from the system control unit 212.
  • the image reconstruction processing unit 206 reconstructs an image on the basis of the selected or collected projection data set.
  • the image reconstruction processing unit 206 may comprise any one of a fan beam reconstruction processing function and a cone beam reconstruction processing function.
  • the image reconstruction processing unit 206 comprises both the fan beam reconstruction processing function and the cone beam reconstruction processing function, and reconstructs an image such as a tomogram by using at least one of the reconstruction processing functions set by the examination plan setting unit 207.
  • the image reconstruction processing unit 206 sequentially reconstructs tomograms by using fan beam reconstruction on the basis of the acquired projection data, in parallel with helical scanning, regardless of a cardiac phase designated and reconstructed by the examination plan setting unit 207 (the above case includes phases other than 65%, i.e., 0 to 100% projection data).
  • the image reconstruction processing unit 206 reconstructs a tomogram (or three-dimensional image) by cone beam reconstruction, after helical scanning or on the background, on the basis of the projection data which is selected for the reconstruction of a tomogram of a cardiac phase as the above reconstruction target. This allows the display unit 210 to display a tomogram almost in real time following helical scanning and display an accurate image based on the tomogram displayed in real time after helical scanning.
  • the X-ray dose is changed (modulated) during scanning. It is, however, difficult for the operator to determine whether the X-ray dose has been changed during scanning.
  • a tomogram can be reconstructed almost in real time.
  • the image SD of a tomogram changes as an X-ray dose is modulated. Since an operator is generally an X-ray engineer, he/she can recognize the modulation of an X-ray dose from a change in the image SD of a tomogram displayed in real time.
  • displaying, on the display unit 210, a tomogram obtained by cone beam reconstruction, which is an accurate tomogram even though it requires a large calculation amount, after scanning makes it possible to perform diagnosis based on the tomogram more accurate than that obtained by the fan beam reconstruction method.
  • Target projection data to be subjected to fan beam reconstruction in parallel with scanning may be projection data acquired by all the detection element rows designated by the examination plan setting unit 207.
  • target projection data is preferably projection data acquired by one detection element row of the X-ray detector 102 (e.g., the middle row in the slice direction, i.e., the 32nd or 33rd row in the middle of a 64-row detector) or the data obtained by adding projection data acquired by a plurality of rows of the X-ray detector 102 (e.g., a plurality of rows in the middle of a multi-row detector in the slice direction, i.e., the 31st, 32nd, 33rd, and 34th rows of the 64-row detector).
  • real-time reconstruction in parallel with scanning may be implemented by reconstructing a tomogram by cone beam reconstruction processing on the basis of data acquired by some detection element rows (one or a plurality of rows) instead of using all the detection element rows in the data acquisition form set by the examination plan setting unit 207.
  • An increase in calculation speed can also be achieved by cone beam reconstruction processing based on data acquired by some detection element rows in this manner.
  • image reconstruction is preferably performed on the basis of projection data by using a reconstruction method called the Feldkamp method.
  • the Feldkamp reconstruction method is an approximate reconstruction method which has been improved on the basis of the fan beam convolution back projection method and is used to generate three-dimensional distribution data of X-ray absorption coefficients (to be referred to as volume data (a stereoscopic (three-dimensional) set of a plurality of voxel data) by handling a target area wide in the slice direction (Z-axis direction) as an aggregate of a plurality of voxels.
  • Cone beam reconstruction processing may be performed such that projection data is three-dimensionally handled and subjected to cone-parallel conversion (rearranged into parallel beams), and three-dimensional back projection is performed on the basis of the rearranged projection data.
  • Fan beam reconstruction processing is performed by using, for example, the fan beam convolution back projection method, and image reconstruction is performed by back projection on the basis of projection data, assuming that an X-ray is perpendicular to the rotation axis of the X-ray tube 101 (the projection data has been obtained by an X-ray in a direction perpendicular to the Z-axis direction).
  • the reconstructed tomogram is temporarily stored in the image storage unit 209 and displayed on the display unit 210.
  • the tomogram is converted into so-called pseudo three-dimensional image data such as a tomogram of an arbitrary slice, a projection image from an arbitrary direction, or a three-dimensional surface image of a specific organ which is obtained by rendering processing in accordance with an instruction from the operator.
  • This data is then displayed on the display unit 210 through the image storage unit 209.
  • the examination plan setting unit 207 comprises a keyboard, various kinds of switches, a mouse, and the like and has a user interface function for allowing the operator to set an examination plan.
  • the examination plan setting unit 207 includes a display unit (which is independent of or incorporated in the display unit 210) for supporting examination planning, and selects/generates an examination plan on a setting window displayed on the display unit 210.
  • Parameters set for an examination plan include an examination target region, a sequence, scanning conditions for the acquisition of data of a subject (patient), reconstruction conditions for image reconstruction, display conditions for the display of a reconstructed image, the voice generation timing at the time of breathing exercise or during scanning, and the like.
  • Examination target regions as setting targets include a head portion, chest portion, abdominal portion, waist portion, lower limbs, and the like. Assume that in this embodiment, a plurality of examination target regions are displayed on a setting window of the examination plan setting unit 207, and the chest portion (the heart if it is included as a selection target) is selected.
  • Sequences that can be selected include a sequence from scanning to image reconstruction, a sequence from scanning to image transfer, sequence from scanning to image recording, and the like.
  • a sequence from scanning to image display is selected by the examination plan setting unit 207.
  • Scan conditions that can be set include a scan type, a data acquisition form indicating an acquisition form for scanning, a reconstruction range, conditions associated with ECG gated scanning, and the like.
  • scanning types the following three types are prepared: conventional scanning, helical scanning, and dynamic scanning.
  • a data acquisition form is represented by "slice count ⁇ slice thickness". Assume that as such forms, two types of conditions, i.e., "64 ⁇ 0.5" and "32 ⁇ 0.5", are stored in advance, and the examination plan setting unit 207 can select one of them.
  • the examination plan setting unit 207 selects "64 ⁇ 0.5", i.e., the form of simultaneously acquiring data of 64 slices by 0.5 mm detection element rows.
  • the data acquisition forms stored in advance are not limited to the above two types of forms, and three or more types of forms may be stored. Obviously, the above numerical values vary depending on the structure of the X-ray detector 102.
  • a reconstruction range is also called a scanning period. Assume that in this embodiment, the start and end positions of such a range are input/set by the examination plan setting unit 207.
  • the examination plan setting unit 207 sets, as conditions associated with ECG gated scanning, a cardiac phase to be reconstructed, a heart rate fluctuation range, an ECG gated reconstruction mode (either half reconstruction or segment reconstruction), a helical pitch, conditions associated with an X-ray dose in a standard scanning period, and the like. Note that no helical pitch is set when conventional scanning or dynamic scanning is selected.
  • a heart rate may be a value per minute or an interval (R-R interval) from a given R wave to the next R wave.
  • a reconstruction cardiac is set in "%” or "msec".
  • the unit “%” is based on the standardization of the interval from a given R wave to the next R wave with 0 to 100% with 0% corresponding to the position of the R wave and 100% corresponding to the position of the next R wave, and expresses a position in the interval.
  • the unit “msec” expresses a delay time (scanning delay time) with reference to the R wave.
  • the examination plan setting unit 207 sets the above data in %
  • the system control unit 212 automatically converts the data into a delay time before scanning
  • the scanning control unit 201 performs control during scanning with reference to a delay time ms.
  • a cardiac phase to be reconstructed is, for example, a central phase which the operator wants to reconstruct, and is set as an arbitrary numerical value by using the keyboard or the like of the examination plan setting unit 207 or by displaying an electrocardiogram acquired before scanning on a display window and making a marking on the electrocardiogram.
  • a set cardiac phase one of phases of 65 to 85% is preferably set to reduce motion artifact.
  • a phase of 75% is set as a cardiac phase to be reconstructed by using the examination plan setting unit 207.
  • a heart rate fluctuation range may be input in the form of numerical values such as 70 to 80 bpm by the operator using the examination plan setting unit 207, or may be set on a graph indicating the relationship between the time and heart rates as shown in FIG. 3A .
  • a heart rate fluctuation range is to be input in the form of numerical values, it is preferable to display a representative value of the heart rate of several heartbeats before scanning (e.g., a median value, average value, maximum heart rate, or minimum heart rate in a breathing exercise, i.e., a voice generation period or at the time of examination plan setting, or a combination thereof) as reference information on a display window. This allows the operator to efficiently set a heart rate fluctuation range. If such a range is to be set by using a graph showing the relationship between the time and heart rates, the range may be displayed parallel to an electrocardiogram as shown in FIG. 3A , or no electrocardiogram may be displayed.
  • a heart rate fluctuation range may be determined in advance as a default range like 80 to 100 bpm instead of being input or set by the operator in the above manner.
  • a heart rate fluctuation range may be automatically determined by the system control unit 212 on the basis of the above representative value of the heart rate of several heartbeats before scanning.
  • the breathing exercise period obtained by the system control unit 212 or the maximum and minimum heart rates at the time of examination plan setting may be determined as a heart rate fluctuation range
  • the maximum and minimum heart rates obtained upon omission of several higher and lower heart rates from heart rates obtained before scanning may be determined as a heart rate fluctuation range
  • a range of 20 or 30 bpm centered on an average or median obtained before scanning may be determined as a heart rate fluctuation range.
  • a heart rate fluctuation range may be determined semi-automatically by making the display unit display, as a default range, a proper heart rate fluctuation range (e.g., maximum and minimum heart rates) of a set of heart rates obtained by the system control unit 212 before scanning, and allowing the operator to edit the displayed range by using a keyboard or the like.
  • a proper heart rate fluctuation range e.g., maximum and minimum heart rates
  • the operator inputs/sets a heart rate fluctuation range in the form of numerical values by using the examination plan setting unit 207.
  • the examination plan setting unit 207 preferably activates a navigation window for setting conditions associated with ECG gated scanning on a display window, and displays at least an input box for a cardiac phase to be reconstructed, an input box for a condition associated with an X-ray dose, a selection box for an ECG gated reconstruction mode (half reconstruction/segment reconstruction), and the above representative value information display box, together with an input box for a heart rate fluctuation range.
  • This allows the operator to identify and input conditions associated with ECG gated scanning and other conditions, and hence makes it possible to prevent operation errors.
  • the conditions associated with an X-ray dose in a standard scanning period include a tube current, a tube voltage, and the like, and the operator inputs numerical values such as a tube voltage of 135 kV and a tube current of 350 mA by using the examination plan setting unit 207.
  • a tube current is controlled by a filament current.
  • a standard scanning period is a period obtained by extending a segment period having a predetermined time width center on a specific cardiac phase with reference to a cardiac cycle used for setting the specific cardiac phase on the basis of the heart rate fluctuation range of a subject.
  • a standard scanning period is a period obtained by extending a segment period set with reference to an average cardiac cycle associated with the subject on the basis of the heart rate fluctuation range of the subject.
  • a segment period is defined as a period during which a projection data set required for the reconstruction of a tomogram is acquired.
  • the start point of a standard scanning period is made to coincide with the start point of a segment period corresponding to the maximum heart rate (the shortest cardiac cycle), and the end point of the standard scanning period is made to coincide with the end point of a segment period corresponding to the minimum heart rate (the longest cardiac cycle).
  • a high dose of X-rays is maintained throughout this standard scanning period. This makes it possible to permit even fluctuations in the heart rate of the subject.
  • a projection data set with a high SNR can be extracted from any time point in the standard scanning period.
  • a tomogram with high image quality can be generated from the projection data set with high SNR.
  • standard scanning period is used. However, this period may be expressed as a first period or the like. Note that a period in a cardiac period except for a standard scanning period will be referred to as a low dose scanning period (or a second period). In the second period, a generation of X-rays may be stopped.
  • the examination plan setting unit 207 may be used to input tube voltages and tube currents in both a standard scanning period and a low X-ray dose scanning period (in this case, control is preferably performed to inhibit a tube current value in a low X-ray dose scanning period from being set to be larger than that in a standard X-ray scanning period).
  • control is preferably performed to inhibit a tube current value in a low X-ray dose scanning period from being set to be larger than that in a standard X-ray scanning period).
  • a tube voltage and tube current in a standard scanning period are set. This makes it possible to prevent the operator from performing erroneous operation and reduce the load imposed on the operator.
  • the examination plan setting unit 207 inputs a reconstruction scheme (fan beam reconstruction/cone beam reconstruction), reconstruction slice thickness, reconstruction interval, and the like as reconstruction conditions. Assume that in this embodiment, cone beam reconstruction is set as a reconstruction scheme.
  • the examination plan setting unit 207 also sets a window level, a window width, and the like as image display conditions.
  • the examination plan set by the examination plan setting unit 207 is transmitted to the system control unit 212.
  • the system control unit 212 has a program for causing the examination plan setting unit 207 to put a set examination plan into practice, and controls the scanning control unit 201, projection data storage unit 203, image reconstruction processing unit 206, and the like. This systematic control by the system control unit 212 implements a sequence from scanning to image reconstruction.
  • the system control unit 212 reads out the electrocardiographic data (electrocardiographic signal) acquired by the electrocardiograph 106 from the projection data storage unit 203 in synchronism with scanning, and extracts, for example, an R wave from the electrocardiographic data.
  • the system control unit 212 also reads out the electrocardiographic data acquired by the electrocardiograph 106 from the projection data storage unit 203, and obtains the heart rate of a plurality of heartbeats.
  • the system control unit 212 further acquires the above representative value (the average of heart rates, the maximum heart rate, the minimum heart rate, or the like) from the heart rate of a plurality of heartbeats.
  • the system control unit 212 determines, on the basis of the cardiac phase to be reconstructed and the heart rate range (heart rate fluctuation range) set by the examination plan setting unit 207, a standard X-ray dose scanning period (the period of a tube current value set when a cardiac phase to be reconstructed and a margin/error range are scanned) during which scanning is performed by using the tube current value set by the examination plan setting unit 207 and a low X-ray dose scanning period (the period of a tube current value smaller than the tube current value in the standard X-ray dose scanning period) during which scanning is performed by using a tube current value smaller than that in the scanning period.
  • a standard X-ray dose scanning period the period of a tube current value set when a cardiac phase to be reconstructed and a margin/error range are scanned
  • a low X-ray dose scanning period the period of a tube current value smaller than the tube current value in the standard X-ray dose scanning period
  • a standard X-ray dose scanning period and low X-ray dose scanning period are preferably calculated in terms of delay times from an R wave.
  • the system control unit 212 may be configured to calculate a standard X-ray dose scanning period and a low X-ray dose scanning period on the basis of the cardiac phase to be reconstructed and the heart rate fluctuation range which are set by the examination plan setting unit 207.
  • the examination plan setting unit 207 is preferably configured to have a storage unit in which standard X-ray dose scanning periods and low X-ray dose scanning periods are stored in association with cardiac phases to be reconstructed and heart rate ranges and to determine a standard X-ray dose scanning period and a low X-ray dose scanning period in accordance with the cardiac phase to be reconstructed and the heart rate fluctuation range which are set by the examination plan setting unit 207.
  • a method of determining a standard X-ray dose scanning period (the period of a set tube current value) and a low X-ray dose scanning period (the period of a low tube current value for modulation) will be described in detail below with reference to FIGS. 2A to 2E .
  • FIG. 2A shows a change in heart rate before scanning, e.g., at the time of breathing exercise.
  • FIG. 2B shows a change in heart rate when a subject is actually scanned.
  • FIG. 2C shows an electrocardiogram of a maximum heart rate, which is obtained before scanning, with reference to an R wave acquired at the time of actual scanning.
  • FIG. 2D shows an electrocardiogram of a minimum heart rate, which is obtained before scanning, with reference to the R wave acquired at the time of actual scanning. Note that each open rectangular mark in FIGS. 2A to 2E indicates a cardiac phase to be reconstructed.
  • the error range of heart rates during a scanning period is predicted from heart rates corresponding to a plurality of periods which are acquired before scanning.
  • the heart rate at the time of breathing exercise changes from 60 bpm to 60 bpm, 83 bpm, 83 bpm, and 90 bpm as shown in FIG. 2A , fluctuations in heart rate at the time of scanning can be predicted such that the maximum heart rate becomes 90 bpm, and the minimum heart rate becomes 60 bpm.
  • a heart rate fluctuation range i.e., a maximum heart rate and a minimum heart rate
  • An R wave is picked up from electrocardiographic information synchronously acquired during scanning.
  • a reconstruction cardiac phase of 75% of a maximum heart rate of 90 bpm is determined as the start position of a standard scanning period
  • a reconstruction cardiac phase of 75% of a minimum heart rate of 60 bpm is determined as the end position of the standard scanning period
  • the remaining cardiac phase is determined as a low X-ray dose scanning period.
  • An X-ray dose or conditions associated with an X-ray dose in a low X-ray dose scanning period may be automatically determined in accordance with the set conditions for the standard scanning period. More specifically, as an X-ray dose or conditions associated with an X-ray dose in the low X-ray dose scanning period, an X-ray dose or conditions associated with an X-ray dose which are about 1/3 to 1/2 that or those in the standard scanning period (if, for example, the set tube current value and set tube voltage value in the standard scanning period are 300 mAs and 135 kV, respectively, a tube current value in the low X-ray scanning period is 1/3 of the set tube current value, i.e., 100 mAs, and a tube voltage value is equal to the set tube voltage value, i.e., 135 kV) are determined in advance. Alternatively, conditions associated with an X-ray dose in the low X-ray dose scanning period are determined to be fixed values (e.g., the tube current value and tube voltage value are determined to be
  • a heart rate fluctuation range may be set by using various kinds of values, e.g., the maximum and minimum heart rates obtained upon omission of several higher and lower heart rates from all the heart rates obtained before scanning, and a predetermined range (for example, 60 to 80 bpm, which are respectively higher and lower than an average of 70 bpm by 10 bmp) from an average or median obtained before scanning.
  • This embodiment has exemplified the case wherein a heart rate fluctuation range can be arbitrarily set by the examination plan setting unit 207. If, however, the range of numerical values input by the operator or the range of a line cursor exceeds a threshold, it is preferable to inhibit the range from being confirmed (inhibit an examination plan from being confirmed) so as to prevent the use of this modulation. This is because since the heart rate fluctuation range of an actual patient hardly exceeds 15 to 30 bpm at the time of scanning, and a patient who exhibits a large heart rate fluctuation range is predicted to have arrhythmia, it is not preferable to use such values without any change.
  • the system control unit 212 supplies an X-ray control signal for controlling the modulation of an X-ray dose to the scanning control unit 201 in accordance with the standard scanning period determined in the above manner or a standard scanning period and a low X-ray dose scanning period. If, for example, the X-ray control signal is at LOW level, a tube voltage and tube current for a low dose are applied from the high voltage generator 104 to the X-ray tube 101 to generate a low dose of X-rays from the X-ray tube 101.
  • the X-ray tube 101 If the X-ray control signal is at HIGH level, since a tube voltage and tube current for a high dose (the tube voltage value and tube current value set by the examination plan setting unit 207 in this case) are applied from the high voltage generator 104 to the X-ray tube 101, the X-ray tube 101 generates a high dose of X-rays.
  • the system control unit 212 sets the X-ray control signal at LOW level in a low X-ray dose scanning period, and sets the X-ray control signal at HIGH level in a standard scanning period. With this operation, X-rays are applied at a low dose in the low X-ray dose scanning period, and are applied at a high dose in the standard scanning period. Even if, therefore, the heart rate of the subject fluctuates during scanning, projection data required to reconstruct a desired cardiac phase can be reliably obtained, and a reduction in exposure during a period irrelevant to diagnosis can be achieved.
  • the system control unit 212 performs control to scan at a high X-ray dose in a standard scanning period and at a low X-ray dose in a low X-ray dose scanning period
  • the tube current or the like (or the X-ray dose) to be supplied from the high voltage generator 104 to the X-ray tube 101 is not abruptly switched from a low X-ray dose scanning period to a standard scanning period. That is, as shown in FIG. 2E , the system control unit 212 gradually changes a tube current or the like (or an X-ray dose) from the high voltage generator 104 in a transition period between a low X-ray dose scanning period and a standard scanning period.
  • the system control unit 212 controls a tube current in a low X-ray dose scanning period so as to prevent the current from becoming equal to or less than a predetermined threshold (tube current value) except when the examination plan setting unit 207 sets otherwise. Such control is performed to prevent failures caused by overloads on the X-ray tube 101 and high voltage generator 104 when a tube current is abruptly increased from a low X-ray dose scanning period to a standard scanning period or abruptly decreased from a standard scanning period to a low X-ray dose scanning period.
  • a predetermined threshold tube current value
  • the system control unit 212 supplies control signals to the scanning control unit 201 to systematically perform rotation control on the rotating frame 103 and movement control on the top 302 in addition to X-ray adjustment control on the scanning control unit 201.
  • the scanning control unit 201 Upon receiving these control signals, the scanning control unit 201 performs various types of control and acquires projection data in accordance with the signals.
  • the projection data is temporarily stored in the projection data storage unit 203 in association with a view, the channel number and row number of the X-ray detector 102, and an electrocardiographic signal (electrocardiographic data).
  • the image reconstruction processing unit 206 sequentially reconstructs tomogram data from the projection data stored in the projection data storage unit 203 by using the fan beam reconstruction method in parallel with scanning, and reconstructs tomogram data in all scanning periods by using the cone beam reconstruction method after the scanning (or on the background).
  • the tomogram data reconstructed by the image reconstruction processing unit 206 is supplied to the display unit 210 through the image storage unit 209 and displayed on the display unit 210.
  • Cardiac examination using the X-ray computed tomography apparatus is roughly performed in the following procedure: breathing exercise, examination plan setting, scanning, image reconstruction, and other processing.
  • the operator makes the subject perform breathing exercise before scanning.
  • breathing exercise the operator attaches an electrode to the subject, and checks whether electrocardiographic signals are accurately acquired by the electrocardiograph 106.
  • the operator makes the subject perform breathing exercise in accordance with a breathing exercise function provided for this apparatus.
  • the operator sets a breath holding period by using the examination plan setting unit 207.
  • a voice guidance like "take in breath", “hold the breath", or "stop it" is generated from the gantry device 1.
  • the electrocardiograph 106 acquires electrocardiographic information in a voice generation period, i.e., a breathing exercise period, and transmits the information to the console 2.
  • the console 2 transmits the received electrocardiographic information to the system control unit 212 through the storage unit 203.
  • the system control unit 212 obtains a heart rate for each period (R wave - R wave interval) in a breathing exercise period.
  • the operator makes an examination plan for cardiac examination by using the examination plan supporting function provided for this apparatus. More specifically, the operator selects the chest portion (the heart if it is included as a selection target) as an examination target region by using the examination plan setting unit 207. If the heart is selected as an examination target region, detailed parameter support information for the heart is displayed on a setting window on the examination plan setting unit 207. The operator inputs scanning conditions, reconstruction conditions, and the like by using the keyboard, mouse, and the like of the examination plan setting unit 207 while referring to this support information.
  • the scan conditions to be input and set include a scanning type (helical scanning in this case), a data acquisition form (simultaneously acquiring 64 slices with 0.5 mm detection element rows/simultaneously acquiring 32 slices with 1.0 mm detection element rows), the start and end positions of a reconstruction range, conditions associated with ECG gated scanning, and the like.
  • the reconstruction conditions to be input include a reconstruction scheme (fan beam reconstruction method/cone beam reconstruction method), a reconstruction slice count, a reconstruction slice thickness, and the like. In this embodiment, as a reconstruction scheme, the cone beam reconstruction method is selected.
  • the conditions associated with ECG gated scanning which are set include a cardiac phase to be reconstructed, a heart rate fluctuation range, a reconstruction mode (half reconstruction/segment reconstruction), a helical pitch, a scanning speed, and conditions (a tube current and a tube voltage) associated with an X-ray dose in a standard scanning range.
  • the system control unit 212 determines a standard X-ray dose scanning period and a low X-ray dose scanning period in accordance with the cardiac phase to be reconstructed and the heart rate fluctuation range which are set by the examination plan setting unit 207.
  • the system control unit 212 obtains a standard X-ray dose scanning period and low X-ray dose scanning period as delay times from an R wave.
  • the operator Upon confirming that the electrocardiograph 106 acquires an electrocardiographic signal, the operator issues an instruction to start examination by using the examination plan setting unit 207.
  • the system control unit 212 controls the scanning control unit 201, projection data storage unit 203, image reconstruction processing unit 206, and the like.
  • the scanning control unit 201 controls the gantry driving device 105 and the bed driving device 301 to make the gantry driving device 105 rotate the rotating frame 103 so as to reach the scanning speed set by the examination plan setting unit 207, and to make the bed driving device 301 move the top 302 to a position immediately before a scanning start position (an approach position for helical scanning).
  • the bed driving device 301 slides the top 302 in the slice direction (Z-axis direction).
  • the high voltage generator 104 supplies the tube voltage and tube current set by the examination plan setting unit 207 to the X-ray tube 101 to apply X-rays.
  • the system control unit 212 When the high voltage generator 104 supplies the tube voltage and the tube current to the X-ray tube 101, the system control unit 212 performs the following processing.
  • the system control unit 212 reads out the electrocardiographic data (electrocardiographic signal) acquired by the electrocardiograph 106 in synchronism with scanning from the storage unit 203, and sequentially picks up R waves from the electrocardiographic data (electrocardiographic signal).
  • the system control unit 212 transmits an X-ray control signal for X-ray dose modulation control to the scanning control unit 201 on the basis of an R wave of the synchronously acquired electrocardiographic signal and delay times from the R wave in the determined standard scanning period and low X-ray dose scanning period.
  • the scanning control unit 201 transmits an X-ray control signal indicating HIGH level so as to apply a high dose of X-rays with a delay time from the R wave in the standard scanning period, and transmits an X-ray control signal indicating LOW level so as to apply a low dose of X-rays with a delay time from the R wave in the low X-ray dose scanning period.
  • the high voltage generator 104 receives an X-ray control signal from the scanning control unit 201, and supplies the tube voltage and tube current set by the examination plan setting unit 207 to the X-ray tube 101 if the signal is at HIGH level. If the X-ray control signal from the scanning control unit 201 is at LOW level, the high voltage generator 104 sets the same tube voltage as that set at HIGH level, and supplies a tube current about 1/3 the tube current value at HIGH level. With this operation, X-rays are applied at a high dose from the X-ray tube 101 in the standard scanning period, and X-rays are applied at a low dose in the low X-ray dose scanning period.
  • a tube current (X-ray dose) gradually decreases in the transition period and becomes a tube current value (X-ray dose) 1/3 that in the low X-ray dose period.
  • the tube current (X-ray dose) gradually decreases in the transition period, and becomes the tube current value (X-ray dose) set in the standard scanning period.
  • the electrocardiograph 106 acquires an electrocardiographic signal in parallel with helical scanning in the data acquisition form set by the examination plan setting unit 207, thereby modulating the X-ray dose during helical scanning.
  • the X-rays transmitted through the subject are detected by the rotating frame 103 and converted into the projection data of an analog electrical signal.
  • the data acquisition device 107 converts this data into the projection data of a digital electrical signal.
  • the data is then sent to the pre-processing unit 202 through a data transmission unit (not shown) to be subjected to various kinds of correction processing.
  • the projection data storage unit 203 of the console 2 stores projection data together with electrocardiographic data (electrocardiographic signal) from the electrocardiograph 106, in association with a view representing the rotation angle of the X-ray tube 101 at the time of data acquisition, a channel number, a row umber, and the like.
  • the image reconstruction processing unit 206 performs real-time reconstruction, in parallel with helical scanning, on the basis of the projection data acquired by some detection element rows, of the data acquisition form (all detection element rows), which are set by the examination plan setting unit 207, to sequentially reconstruct tomograms, and the display unit 210 displays the sequentially reconstructed tomograms.
  • the image reconstruction processing unit 206 weights data associated with a cardiac phase to be reconstructed which is designated by the examination plan setting unit 207 (in this case, projection data of the same cardiac phase which are acquired by segment reconstruction) after helical scanning or on the background, and reconstructs a plurality of tomograms in the reconstruction range set by the examination plan setting unit 207 by using cone beam reconstruction with a set image pitch and a set image slice thickness.
  • the display unit 210 then displays a tomogram obtained by cone beam reconstruction.
  • an X-ray dose is to be demodulated in ECG gated scanning
  • scanning is performed under set X-ray conditions in a margin period as well as in a period required for the reconstruction of a designated cardiac phase to be reconstructed.
  • This makes it possible to obtain the projection data of the cardiac phase to be reconstructed at the X-ray dose designated by the operator (i.e., an image with a desired S/N) while reducing the exposure to the subject even if the heart rate (R-R interval) of the subject fluctuates.
  • scanning can be performed upon prediction of fluctuations in heart rate at the time of scanning, i.e., an error range, by determining a standard scanning period on the basis of a plurality of heart rates acquired before scanning and the cardiac phase to be reconstructed which is designated by the operator. This makes it possible to reliably obtain the data of the cardiac phase to be reconstructed which is desired by the operator while a reduction in exposure to the subject is achieved.
  • a standard scanning period is determined on the basis of a plurality of heart rates in a breathing exercise period. Since the subject holds his/her breath in a breathing exercise period at the time of scanning, a heart rate fluctuation range can be accurately predicted.
  • maximum and minimum heart rates are picked up from a plurality of heart rates acquired before scanning and are used as a heart rate fluctuation range, thereby increasing the prediction accuracy of the heart rate fluctuation range at the time of scanning.
  • real-time reconstruction is performed, in parallel with helical scanning, on the basis of the projection data acquired by some detection element rows, of all the detection element rows of the data acquisition form, which are set by the examination plan setting unit 207, to sequentially reconstruct tomograms, and the display unit 210 displays the sequentially reconstructed tomograms.
  • a tomogram is reconstructed by using cone beam reconstruction after the end of helical scanning or on the background on the basis of projection data associated with the cardiac phase to be reconstructed which is designated by the examination plan setting unit 207. This allows the operator to check a tomogram in real time, and hence the operator can check on the basis of a change in image SD whether the X-ray dose is modulated. In addition, after the scanning, diagnosis can be performed with an accurate tomogram.
  • providing a transition period between a standard scanning period and a low X-ray dose scanning period and providing a limitation to inhibit a tube current in a low X-ray dose scanning period from becoming equal to or less than a given value makes it possible to prevent an excessive load from being imposed on the X-ray tube 101 and the like and prevent failures.
  • constituent elements can be variously modified and embodied at the execution stage within the spirit and scope of the invention.
  • Various inventions can be formed by proper combinations of a plurality of constituent elements disclosed in the above embodiments. For example, several constituent elements may be omitted from the all the constituent elements in the embodiment.
  • scanning is performed at the X-ray dose based on the set X-ray conditions in a standard scanning period, and scanning is performed at a lower X-ray dose in a low X-ray does scanning period than in the standard scanning period (set X-ray conditions).
  • X-rays applied to a subject in a low X-ray dose scanning period may be stopped/shielded, or the low X-ray dose scanning period may be provided with a period in which the X-ray dose is 0.
  • a heart rate fluctuation range is set by the examination plan setting unit 207 and is determined by the system control unit 212.
  • This makes it possible to perform scanning at a high X-ray dose to a slightly excessive extent for data required for a reconstruction central phase in at least one heart rate. Even if, therefore, slight heart rate fluctuations occur during scanning, an image of a desired reconstruction central phase can be reconstructed while a reduction in exposure is achieved, thereby saving the labor of inputting/setting a heart rate fluctuation range.
  • a heart rate fluctuation range (or more directly, a standard scanning period) on the basis of the heart rate of one or more heartbeats acquired during scanning instead of setting a heart rate fluctuation range from electrocardiographic information before scanning, for example, at the time of breathing exercise.
  • a heart rate fluctuation range may be determined in accordance with pieces of electrocardiographic information both before scanning and during scanning. If the heart rate obtained in accordance with electrocardiographic information acquired in parallel with scanning exceeds the heart rate fluctuation range determined before scanning, the X-ray dose based on the set tube current and tube voltage is maintained without X-ray modulation even during scanning. This makes it possible to obtain the data of a cardiac phase to be reconstructed even if arrhythmia or the like occurs in the patient during scanning.
  • a heart rate as a reference with which a heart rate fluctuation range is automatically set may be an average value or median value instead of a maximum heart rate or a minimum heart rate.
  • a slight margin e.g., several % or several msec
  • a standard scanning period without setting a period which one-to-one corresponds to a cardiac phase to be reconstructed in a heart rate fluctuation range (e.g., a maximum heart rate and a minimum heart rate).
  • the system control unit 212 determines a standard scanning period as follows.
  • the system control unit 212 calculates the heart rate or electrocardiogram designated by the operator as the maximum heart rate and a heart rate lower than the maximum heart rate by 10 to 20 bpm as the minimum heart rate, and determines the time corresponding to the maximum heart rate as the start time of the standard scanning period and the time corresponding to the minimum heart rate as the end time of the standard scanning period.
  • the operator calculates the heart rate or electrocardiogram designated by the operator as the minimum heart rate and a heart rate higher than the minimum heart rate by 10 to 20 bpm as the maximum heart rate, and determines the time corresponding to the minimum heart rate as the end time of the standard scanning period and the time corresponding to the calculated maximum heart rate as the start time of the standard scanning period.
  • the X-ray dose in the standard scanning period may be changed in a plurality of steps.
  • slightly high X-ray doses are set for predetermined views (e.g., 45° - 135° and 225° - 270°) in a standard scanning period
  • slightly low X-ray does are set for other views (e.g., 315° - 45° and 135° - 225°)
  • tube current values are set for other views (e.g., 315° - 45° and 135° - 225°)
  • a tube current value in a low X-ray dose scanning period is determined on the basis of a set tube current value in a standard scanning period or is set by the examination plan setting unit 207.
  • the present invention is not limited to this. Assume that pre-scanning is to be performed to obtain a contrast medium injection timing before scanning of the heart, that is, a tomogram is reconstructed in real time on the basis of projection data obtained by monitoring scanning on the upstream side of the heart (e.g., the cervical region) for which a dose lower than that for scanning of the heart is set, and a value increasing from a CT value or mask image is to be displayed on the display unit 210.
  • the tube current value in the low X-ray dose scanning period changes between a set tube current value in the standard scanning period as an upper limit and a tube current value in the low X-ray dose scanning period as a lower limit. This makes it unnecessary for the operator to determine three kinds of tube current values in a standard scanning period, monitoring scanning period, and low X-ray dose scanning period, thereby reducing the labor of the user in setting X-ray conditions.
  • segment reconstruction is performed by acquiring segments (patches) corresponding to two or more heartbeats.
  • segments patterns
  • projection data corresponding to half scanning 180° + fan angle
  • the third heartbeat overlaps part of the first heartbeat and part of the second heartbeat.
  • X-rays are applied in a cardiac phase at the third heartbeat to acquire the projection data of the segment corresponding to the fourth heartbeat.
  • the system control unit 212 performs control to perform scanning with the tube current value in a standard scanning period with respect to the three segments (cardiac phases) corresponding to the first, second, and fourth heartbeats and perform scanning with a tube current value for low dose scanning with respect to the segment (cardiac phase) corresponding to the third heartbeat. That is, when the overlapping portions between segments in segment reconstruction are large, the system control unit 212 determines a low X-ray dose scanning period for at least one segment (cardiac phase) instead of a standard scanning period.
  • At least one of the plurality of times of acquisition is determined as a low X-ray dose scanning period instead of a standard scanning period. This makes it possible to further reduce exposure of the subject.
  • X-ray computed tomography apparatuses include various types of apparatuses, e.g., a rotate/rotate-type apparatus in which an X-ray tube and X-ray detector rotate together around a subject to be examined, and a stationary/rotate-type apparatus in which many detection elements are arrayed in the form of a ring, and only an X-ray tube rotates around a subject to be examined.
  • the present invention can be applied to either type. In this case, the rotate/rotate type, which is currently the mainstream, will be exemplified.
  • reconstruction methods include the full reconstruction method, half reconstruction method, and segment reconstruction method. These reconstruction methods differ in angle range required to reconstruct one-slice tomogram data. Note that the time required for the X-ray tube to rotate throughout the angle range required for the reconstruction of one-slice tomogram data is called time resolution.
  • the full reconstruction method projection data acquired while the X-ray tube rotates through 360° is required to reconstruct one-slice tomogram data.
  • the half reconstruction method projection data acquired while the X-ray tube rotates through (180° + ⁇ ) is required to reconstruct one-slice tomogram data. Note that ⁇ represents the spreading angle of X-rays, i.e., a fan angle.
  • the segment reconstruction method is a method of preparing (180° + ⁇ ) projection data by acquiring projection data in the range of ((180/n)° + ⁇ /n), where n is the number of segments, from continuous or discrete n cardiac cycles.
  • Time resolution in this segment reconstruction method is given as the time required for the X-ray tube to rotate throughout the angle range of ⁇ (180/n)° + ⁇ /n).
  • the present invention can be applied to either reconstruction scheme. In this case, the half scanning method will be exemplified.
  • an indirect conversion type that converts X-rays into light through a phosphor such as a scintillator and converts the light into electric charges through photoelectric conversion elements such as photodiodes
  • a direct conversion type that uses generation of electron-hole pairs in a semiconductor by X-rays and migration of the electron-hole pairs to an electrode, i.e., a photoconductive phenomenon.
  • An X-ray detection element can employ either of these schemes.
  • the former type i.e., the indirect conversion type, will be exemplified.
  • the present invention can be applied to both a conventional single-tube type X-ray computed tomography apparatus and a multi-tube type X-ray computed tomography apparatus.
  • the single-tube type X-ray computed tomography apparatus will be exemplified here.
  • FIG. 5 shows the arrangement of an X-ray computed tomography apparatus according to this embodiment.
  • This X-ray computed tomography apparatus includes a gantry 1 configured to acquire projection data associated with a subject to be examined.
  • the gantry 1 includes an X-ray tube 10 and a multi-channel X-ray detector 23.
  • the X-ray tube 10 and the multi-channel X-ray detector 23 are mounted on an annular rotating frame 12 rotated/driven by a gantry driving device 25 so as to face each other through an opening portion in a central portion.
  • a subject P placed on a top 2a of a bed 2 is inserted into the opening portion.
  • An electrocardiograph 22 is attached to the subject P to detect an electrocardiogram of the subject P.
  • the multi-channel X-ray detector 23 is placed adjacent to a reference X-ray detector 24. X-rays which are not transmitted through the subject are applied to the reference X-ray detector 24.
  • the reference X-ray detector 24 detects the output intensity of X-rays which have been generated from the X-ray tube 10 and have been hardly attenuated, and generates the resultant data (to be referred to as X-ray output data).
  • the reference X-ray detector 24 can be replaced by another constituent element which can generate X-ray output data representing the output intensity of X-rays, e.g., an ammeter (11-1 in FIG. 6 ) which measures the tube current of the X-ray tube 10 or an ammeter (11-2 in FIG. 6 ) which measures the filament current of the X-ray tube 10.
  • a tube voltage generating unit 21-1 of a high voltage generator 21 applies a high voltage (tube voltage) between a cathode 10-3 and an anode 10-2 which are placed in a vacuum in a glass tube 10-1.
  • a filament current is supplied from a filament current generating unit 21-2 of the high voltage generator 21 to a filament 10-4 of the X-ray tube 10.
  • the thermoelectrons generated upon supply of the filament current are accelerated under high voltage and collide with the tungsten target of the anode 10-2, thereby generating X-rays.
  • a data acquisition device 26 generally called a DAS (Data Acquisition System) converts a signal output from the X-ray detector 23 for each channel into a voltage signal, amplifies it, and further converts it into a digital signal.
  • This data (also called raw data) is supplied to a computer unit 3 placed outside the gantry.
  • a pre-processing unit 34 of the computer unit 3 performs correction processing such as sensitivity correction for the data (raw data) output from a data acquisition unit 26.
  • This projection data is sent to a projection data storage device 37 of the computer unit 3 and is stored together with a time code. Electrocardiographic data from the electrocardiograph 22 is also stored in the projection data storage device 37.
  • the computer unit 3 comprises a system controller 29, input device 39, display 38, scanning controller 30, reconstruction unit 36, R wave detecting unit 42, X-ray output control expert system 43, and X-ray output data storage unit 41.
  • the reconstruction unit 36 corresponds to any of full reconstruction processing, half reconstruction processing, and segment reconstruction processing, the unit will be described as the one for half reconstruction processing.
  • the R wave detecting unit 42 includes a function of typically detecting an R wave as a characteristic wave from the electrocardiogram data obtained by the electrocardiograph 22, and a function of repeatedly measuring the heart rate of the subject P on the basis of the period of the R wave.
  • the X-ray output data storage unit 41 stores the X-ray output data generated by the reference X-ray detector 24, together with a time code.
  • the X-ray output control expert system 43 has a function of setting a specific period in a cardiac cycle of a subject in time (msec) expression in accordance with a cardiac phase to be subjected to image reconstruction which is designated in percent expression by the operator through the input device 39, a function of performing extension processing for this specific period on the basis of a time width (time resolution) corresponding to the angle range of projection data required for image reconstruction and the rise time of X-rays, and a function of supplying data in the specific period having undergone the extension processing to the scanning controller 30.
  • the scanning controller 30 executes ECG gated scanning on the basis of the data in the specific period having undergone the extension processing.
  • X-rays are generated from the X-ray tube 10 with reference to the R wave of the electrocardiogram, and stops the generation of X-rays in a period other than the specific period.
  • the X-ray tube 10 generates X-rays at a relatively high intensity in the specific period with reference to the R wave of the electrocardiogram and generates X-rays at a relatively low intensity in a period other than the specific period.
  • the generation/stop of X-rays or the modulation of X-rays is controlled by either a tube voltage or a filament current or a combination thereof. Control of the modulation of X-rays will be exemplified. In a period except for the specific period, a generation of X-rays may be stopped
  • the above rise time of X-rays is defined as the time required for the intensity of X-rays to reach from an almost zero value to, for example, 90% of a predetermined intensity value (relatively high output value) or the time required for the intensity of X-rays to reach from a predetermined relatively low intensity value to, for example, 90% of a predetermined intensity value (relatively high output value).
  • the latter will be exemplified here.
  • the subject executes a breath holding trial (exercise) in a preparatory stage before scanning (S11) under the control of the system controller 29.
  • An electrocardiogram in a period including at least the breath holding trial period is measured by the electrocardiograph 22.
  • An R wave is detected by the R wave detecting unit 42 on the basis of the electrocardiogram (S12).
  • the R wave detecting unit 42 detects an R wave and measures the interval between R waves as a cardiac cycle to specify a shortest cardiac cycle and a longest cardiac cycle in the breath holding trial period.
  • the electrocardiogram is displayed on the display 38 as shown in FIG. 9 . On this window, at least two cardiac phases, i.e., the first and second cardiac phases, are designated through the input device 39 (S13).
  • the period from the first cardiac phase to the second cardiac phase is a period in which it is desired to acquire projection data with a high S/N ratio and perform image reconstruction with high image quality.
  • a cardiac phase is designated in percentage (%) with the overall period of a single cardiac cycle being regarded as 100%. For example, 30% and 80% are designated.
  • the X-ray output control expert system 43 converts the period designated in percentage into an elapsed time (msec) from the R wave.
  • the elapsed time (to be referred to as the first time) from the R wave which corresponds to the first cardiac phase (e.g., 30%) is determined from the shortest cardiac cycle (S14).
  • the elapsed time (to be referred to as the second time) from the R wave which corresponds to the second cardiac phase (e.g., 80%) is determined from the longest cardiac cycle (S15).
  • the X-ray output control expert system 43 then quickens the start point (first time) of the period (specific period) from the first time to the second time which is expressed in msec and in which it is desired to perform image reconstruction with high image quality by 1/2 a time (time resolution) " ⁇ t(180 + ⁇ ) required to reconstruct one-slice tomogram data, i.e., the time required for the X-ray tube 10 to rotate through (180° + ⁇ ) (S16).
  • the X-ray output control expert system 43 further quickens the first time by a predetermined rise time of X-rays (S17).
  • the X-ray output control expert system 43 delays the end point (second time) of the period (specific period) from the first time to the second time which is expressed in msec and in which it is desired to perform image reconstruction with high image quality by a time corresponding to 1/2 the time resolution " ⁇ t(180 + ⁇ )" (S18).
  • the start point and end point of a specific period are determined from the shortest cardiac cycle and longest cardiac cycle, respectively, and the specific period is extended on the basis of time resolution and the rise time of X-rays. This makes it possible to reduce the occurrence of a situation in which in ECG gated scanning, projection data required for image reconstruction of a desired cardiac phase has not been acquired or projection data has not been acquired with a relatively high S/N ratio.
  • the X-ray output control expert system 43 displays, on the same time axis on the electrocardiogram in a breath holding trial period, the period (the data range required for reconstruction) from the first time determined in step S16 to the second time determined in step S18 and the period (expected X-ray high output period) from the first time determined in step S17 to the second time determined in step S18.
  • the former period is a period required for high-quality images
  • the latter period is an expected period in which X-rays are output at a high intensity.
  • the operator can check the mismatch between the two periods on a window. The operator can extend or shorten the expected period in which X-rays are output at a high intensity, as needed, by operating the input device 39.
  • a period (a range in which high-quality images are required) specified by the percentage designated from the electrocardiogram of the subject or a specific waveform sequence may be displayed instead of the period (data range required for reconstruction) from the first time determined in step S16 to the second time determined in step S18.
  • the X-ray output control expert system 43 supplies data associated with the period from the first time to the second time which is determined by the X-ray output control expert system 43 to the scanning controller 30.
  • the scanning controller 30 starts ECG gated scanning upon operation of a trigger button mounted on the input device 39 (S19).
  • the scanning controller 30 performs X-ray modulation control during ECG gated scanning.
  • the scanning controller 30 modulates X-rays from low output to high output when a predetermined period of time has elapsed from the R wave pulse detected by the R wave detecting unit 42 and the first time is reached, and continues the high output state when a predetermined period of time has elapsed from the R wave pulse and the second time is reached.
  • the scanning controller 30 modulates X-rays from high output to low output when a predetermined period of time has elapsed from the R wave pulse detected by the R wave detecting unit 42 and the second time is reached.
  • Such X-ray output modulation control is repeated for each cardiac cycle.
  • the projection data acquired by the data acquisition device 26 during the continued ECG gated scanning period is sent to the projection data storage device 37 of the computer system 3 and stored, together with a time code.
  • the electrocardiogram data obtained by the electrocardiograph 22 is also stored in the projection data storage device 37.
  • the X-ray output data generated by the reference X-ray detector 24 is stored in the X-ray output data storage unit 41, together with a time code (S21).
  • the scanning controller 30 stops subsequent X-ray output modulation control (S22).
  • a predetermined upper heart rate e.g. 19 ppm
  • the scanning controller 30 stops subsequent X-ray output modulation control (S22).
  • S22 X-ray output modulation control
  • the heart rate in a cardiac cycle Sn immediately before the current time is 48
  • the heart rate in an immediately preceding cardiac cycle Sn-1 is 68
  • their heart rate difference "20" exceeds the upper limit heart rate difference "19”.
  • X-ray output modulation control is stopped from a subsequent cardiac cycle Sn+1, and X-rays are steadily maintained at a high output level. This stop control can prevent data omission even if arrhythmia occurs.
  • the X-ray output control expert system 43 displays the electrocardiographic data stored in the projection data storage device 37, and displays, on the same time axis in accordance with a time code, the period (the data range required for reconstruction) from the first time determined in step S16 to the second time determined in step S18 and the period (the period in which high image quality is maintained) which is specified on the basis of the X-ray output data stored in the X-ray output data storage unit 41 in step S21 and in which X-rays are actually output at a high output level (S24).
  • the X-ray output control expert system 43 may display the period (the range in which high-quality images are required) specified by the percentage designated from an electrocardiogram of the subject or a specific waveform sequence instead of the period (the data range required for reconstruction) from the first time determined in step S16 to the second time determined in step S18.
  • the X-ray output control expert system 43 automatically detects that a cardiac cycle which is specified for each cardiac cycle from the percentage designated in step S13 and in which a high-quality image is desired deviates at least partly from the X-ray high output period (the period in which high image quality is maintained) which is specified on the basis of the X-ray output data stored in the X-ray output data storage unit 41 in step S21 (S25). Alternatively, the operator can determine the corresponding cardiac cycle and automatically designate it.
  • the reconstruction unit 36 excludes projection data acquired in the detected cardiac cycle, and performs image reconstruction (S26).
  • This embodiment can reduce the occurrence of a situation in which projection data required for image reconstruction of a desired cardiac phase has not been acquired or projection data has not been acquired with an expected relatively high S/N ratio.

Claims (18)

  1. Dispositif de tomographie aux rayons X comprenant :
    une source de rayons X (101) adaptée pour générer des rayons X ;
    un détecteur de rayons X (102) adapté pour détecter des rayons X transmis à travers un sujet à examiner pour générer des données de projection ;
    une unité de stockage (203) adaptée pour stocker les données de projection en association avec des données électrocardiographiques du sujet ;
    une unité de réglage (212) adaptée pour définir une phase cardiaque spécifique dans un cycle cardiaque en fonction des instructions d'un opérateur ;
    une unité d'établissement de plan d'examen (207) adaptée pour établir une plage de fluctuation de fréquence cardiaque ;
    une unité de reconstruction (206) adaptée pour reconstruire une image sur la base d'une pluralité d'ensembles de données de projection acquise dans une période prédéterminée centrée sur la phase cardiaque spécifique et sélectionnée parmi des cycles cardiaques continus ;
    une unité de détermination (212) adaptée pour déterminer une période de balayage de dose de rayons X standard dans laquelle le sujet est balayé par une dose élevée de rayons X ;
    et
    une unité de commande (212) adaptée pour contrôler un courant de tube de la source de rayons X pour générer une dose relativement élevée de rayons X dans la période de balayage de dose de rayons X standard et générer une dose relativement faible de rayons X ou arrêter une génération de rayons X dans une période de balayage à faible dose de rayons X,
    dans lequel la phase cardiaque spécifique et une plage de fluctuation de fréquence cardiaque sont converties en temps de retard par rapport à une onde R, et
    l'unité de commande (212) est adaptée pour contrôler le courant de tube de la source de rayons X avec les temps de retard convertis ;
    caractérisé par le fait que la détermination de la période de balayage de dose de rayons X standard est basée sur la phase cardiaque spécifique et la plage de fluctuation de fréquence cardiaque, de sorte que la phase cardiaque spécifique est incluse dans la période de balayage de dose de rayons X standard si une fréquence cardiaque du sujet varie dans la plage de fluctuation de fréquence cardiaque.
  2. Dispositif selon la revendication 1, caractérisé par le fait que la plage de fluctuation de fréquence cardiaque est déterminée sur la base d'une fréquence cardiaque correspondant à une pluralité de battements cardiaques.
  3. Dispositif selon la revendication 1, caractérisé par le fait que la plage de fluctuation de fréquence cardiaque est déterminée conformément à une instruction d'opérateur.
  4. Dispositif selon la revendication 1, caractérisé par le fait que la plage de fluctuation de fréquence cardiaque est déterminée sur la base d'une valeur typique d'une pluralité de fréquences cardiaques obtenues avant l'acquisition des données de projection.
  5. Dispositif selon la revendication 2, caractérisé par le fait que l'unité de détermination est adaptée pour prolonger chacune des périodes spécifiques sur la base de la plage de fluctuation de fréquence cardiaque du sujet ; et
    un point de départ de la période étendue est défini sur un point de départ d'une période correspondant à la fréquence cardiaque maximale, et un point final de la période de balayage de dose de rayons X standard est défini sur un point final d'une période correspondant à la fréquence cardiaque minimale.
  6. Dispositif selon la revendication 5,
    caractérisé par le fait que l'unité de commande est adaptée pour contrôler un courant de tube de la source de rayons X afin de moduler un courant de tube devant être fourni par l'unité de génération de haute tension à la source de rayons X dans la période spécifique de balayage de dose de rayons X standard et ladite période de balayage à faible dose de rayons X
  7. Dispositif selon la revendication 6,
    caractérisé par le fait que l'unité de commande est adaptée pour déterminer une valeur de courant de tube dans la période spécifique de balayage de dose de rayons X standard conformément à une instruction d'opérateur, et pour déterminer une valeur de courant de tube dans ladite période de balayage à faible dose de rayons X sur la base de la valeur du courant de tube dans la période spécifique de balayage de dose de rayons X standard.
  8. Dispositif selon la revendication 6,
    caractérisé par le fait que l'unité de commande est conçue pour fournir, entre la période spécifique de balayage de dose de rayons X standard et ladite période de balayage à faible dose de rayons X, une période de transition d'une valeur de courant de tube entre la valeur de courant de tube dans la période spécifique de balayage de dose de rayons X standard et la valeur de courant de tube dans ladite période de balayage à faible dose de rayons X.
  9. Dispositif selon la revendication 3, caractérisé par le fait qu'il comprend en outre
    une unité d'affichage adaptée pour afficher un graphique représentant un changement temporel de la fréquence cardiaque avant le balayage, et
    une unité d'opération pour désigner une plage de fluctuation de fréquence cardiaque sur le graphique.
  10. Dispositif selon la revendication 9,
    caractérisé par le fait que l'unité d'affichage est conçue pour afficher un graphique indiquant une relation entre un temps partiel comprenant au moins une fréquence cardiaque maximale et une fréquence cardiaque minimale, et un électrocardiogramme dans une période correspondant au graphique.
  11. Dispositif selon l'une quelconque des revendications 1 à 10, caractérisé par le fait que l'unité de commande est adaptée pour contrôler le courant de tube pour générer la dose élevée des rayons X dans ladite période de balayage à faible dose de rayons X lorsqu'une fréquence cardiaque obtenue parallèlement à l'acquisition des données de projection dévie de la plage de fluctuation de fréquence cardiaque.
  12. Dispositif selon l'une quelconque des revendications 1 à 10, caractérisé par le fait que l'unité de commande est adaptée pour commander l'unité de génération de haute tension pour changer une valeur de courant de tube dans ladite période de balayage à faible dose de rayons X dans une plage d'une valeur de courant de tube dans la période spécifique et d'une valeur de courant de tube dans une période de pré-balayage lorsque le pré-balayage est effectué pour obtenir une synchronisation d'injection de produit de contraste avant l'acquisition des données de projection.
  13. Dispositif selon l'une quelconque des revendications 1 à 12, caractérisé par le fait que l'unité de reconstruction est adaptée pour pondérer et ajouter des données de projection avec la même vue entre ladite pluralité d'ensembles de données de projection.
  14. Dispositif selon la revendication 13,
    caractérisé par le fait que l'unité de reconstruction est adaptée pour appliquer aux données de projection ayant la même vue un poids correspondant à une fréquence cardiaque dans un cycle cardiaque au cours duquel les données de projection sont acquises.
  15. Dispositif selon la revendication 14,
    caractérisé par le fait qu'un poids appliqué aux données de projection acquises dans un cycle cardiaque dans lequel la fréquence cardiaque est relativement élevée est inférieur à un poids appliqué aux données de projection acquises dans un cycle cardiaque dans lequel la fréquence cardiaque est relativement faible.
  16. Dispositif selon la revendication 13,
    caractérisé par le fait que l'unité de reconstruction est adaptée pour appliquer aux données de projection ayant la même vue un poids correspondant à un taux d'occupation desdits chaque ensemble de données de projection à une plage angulaire nécessaire à la reconstruction d'image.
  17. Dispositif selon la revendication 16,
    caractérisé par le fait que le poids à appliquer aux données de projection dans un ensemble de données de projection qui est relativement élevé dans le rapport est plus lourd qu'un poids à appliquer aux données de projection dans un ensemble de données de projection qui est relativement faible dans le rapport.
  18. Dispositif selon l'une quelconque des revendications 1 à 17, caractérisé par le fait que les données de projection sont acquises par balayage hélicoïdal et
    l'unité de reconstruction est conçue pour reconstruire séquentiellement des tomogrammes par reconstruction en temps réel sur la base d'au moins une partie des données de projection obtenue par le détecteur de rayons X en parallèle avec le balayage hélicoïdal, et reconstruire une image par reconstruction de faisceau conique sur la base de données de projection après la fin du balayage hélicoïdal.
EP06018572.5A 2005-09-07 2006-09-05 Dispositif de tomographie aux rayons x Active EP1762176B1 (fr)

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EP12152086A EP2449969A1 (fr) 2005-09-07 2006-09-05 Dispositif de tomographie aux rayons X
EP12152088.6A EP2449970B1 (fr) 2005-09-07 2006-09-05 Dispositif de tomographie aux rayons X
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EP12152088.6A Division-Into EP2449970B1 (fr) 2005-09-07 2006-09-05 Dispositif de tomographie aux rayons X
EP12152088.6A Division EP2449970B1 (fr) 2005-09-07 2006-09-05 Dispositif de tomographie aux rayons X
EP12152086A Division-Into EP2449969A1 (fr) 2005-09-07 2006-09-05 Dispositif de tomographie aux rayons X
EP10170123.3A Division-Into EP2238906B1 (fr) 2005-09-07 2006-09-05 Dispositif de tomographie aux rayons X
EP10170123.3A Division EP2238906B1 (fr) 2005-09-07 2006-09-05 Dispositif de tomographie aux rayons X
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JP5726050B2 (ja) 2015-05-27
EP1762176A3 (fr) 2009-12-02
EP2452626B1 (fr) 2013-09-04
EP2449968A1 (fr) 2012-05-09
JP2012035126A (ja) 2012-02-23
EP2449969A1 (fr) 2012-05-09
EP2449970B1 (fr) 2021-03-24
JP5619707B2 (ja) 2014-11-05
US7715520B2 (en) 2010-05-11
EP2238906A1 (fr) 2010-10-13
EP2238906B1 (fr) 2015-04-08
EP2452626A1 (fr) 2012-05-16
JP2012061324A (ja) 2012-03-29
EP1762176A2 (fr) 2007-03-14
JP2012061325A (ja) 2012-03-29
JP5454961B2 (ja) 2014-03-26
US20070053483A1 (en) 2007-03-08
EP2449968B1 (fr) 2021-11-10
EP2449970A1 (fr) 2012-05-09
JP5726051B2 (ja) 2015-05-27

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